Galantamine
- Product NDC
- 0904-7104
- 11-digit product format
- 009047104
- Labeler code
- 0904
- Product ID
- 0904-7104_47dec5b0-d625-46f9-9363-4a0274035eaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077604
- Marketing category
- ANDA
- Marketing start
- 2017-08-02
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7104-04 | 00904710404 | 30 BLISTER PACK in 1 CARTON (0904-7104-04) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2017-08-02 | 0000-00-00 | No | No | Current |